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Preview	Issue Date	Title	Author(s)
	2007	SCN2A mutations and benign familial neonatal-infantile seizures: The phenotypic spectrum	Herlenius, E.; Heron, S.; Grinton, B.; Keay, D.; Scheffer, I.; Mulley, J.; Berkovic, S.
	2007	A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy	Cavalleri, G.; Walley, N.; Soranzo, N.; Mulley, J.; Doherty, C.; Kapoor, A.; Depondt, C.; Lynch, J.; Scheffer, I.; Heils, A.; Gehrmann, A.; Kinirons, P.; Gandhi, S.; Satishchandra, P.; Wood, N.; Anand, A.; Sander, T.; Berkovic, S.; Delanty, N.; Goldstein, D.; et al.
	2006	Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults	Jansen, F.; Sadleir, L.; Harkin, L.; Vadlamudi, L.; McMahon, J.; Mulley, J.; Scheffer, I.; Berkovic, S.
	2004	Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction	Richards, M.; Heron, S.; Spendlove, H.; Scheffer, I.; Grinton, B.; Berkovic, S.; Mulley, J.; Davy, A.
	2007	Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures	Heron, S.; Cox, K.; Grinton, B.; Zuberi, S.; Kivity, S.; Afawi, Z.; Straussberg, R.; Berkovic, S.; Scheffer, I.; Mulley, J.
	2002	X-linked myoclonic epilepsy with spasticity and intellectual disability - Mutation in the homeobox gene ARX	Scheffer, I.; Wallace, R.; Phillips, F.; Hewson, P.; Reardon, K.; Parasivam, G.; Stromme, P.; Berkovic, S.; Gecz, J.; Mulley, J.
	2004	Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsy	Tan, N.; Heron, S.; Scheffer, I.; Pelekanos, J.; McMahon, J.; Vears, D.; Mulley, J.; Berkovic, S.
	2003	Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms	Wallace, R.; Hodgson, B.; Grinton, B.; Gardiner, R.; Robinson, R.; Rodriguez-Casero, V.; Sadleir, L.; Morgan, J.; Harkin, L.; Dibbens, L.; Yamamoto, T.; Andermann, E.; Mulley, J.; Berkovic, S.; Scheffer, I.
	2006	A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A	Mulley, J.; Nelson, P.; Guerrero, S.; Dibbens, L.; Iona, X.; McMahon, J.; Harkin, L.; Schouten, J.; Yu, S.; Berkovic, S.; Scheffer, I.
	2010	Detection of microchromosomal aberrations in refractory epilepsy: a pilot study	McMahon, J.; Scheffer, I.; Nicholl, J.; Waters, W.; Eyre, H.; Hinton, L.; Wilson, P.; Yu, S.; Dibbens, L.; Berkovic, S.; Mulley, J.